Myopathy in hypophosphataemic osteomalacia presenting in adult life.
Three cases of hypophosphataemic osteomalacia presenting in adult life, in which a myopathy was a prominent presenting feature, are described. In one, a nasopharyngeal haemangioma was also present. Possible mechanisms underlying the myopathy are discussed briefly.
Gespeichert in:
| Veröffentlicht in: | J Neurol Neurosurg Psychiatry |
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| Hauptverfasser: | , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BMJ Publishing Group
1975
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| Schlagworte: | |
| Online-Zugang: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC491911/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1151410/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jnnp.38.3.297 |
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